Company ยท US
Airos Medical, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2024. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| JOW | Sleeve, Limb, Compressible | 7 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 11, 2024 | K240499 | ARTAIRA Arterial Compression Device (AACD01) Airos Medical, Inc. | JOW |
| Dec 9, 2022 | K223195 | AIROS 6P Sequential Compression Device Airos Medical, Inc. | JOW |
| Dec 9, 2022 | K223193 | AIROS 8P Sequential Compression Device Airos Medical, Inc. | JOW |
| Dec 4, 2019 | K193069 | AIROS 6 Sequential Compression Device Airos Medical, Inc. | JOW |
| Dec 4, 2019 | K193068 | AIROS 8 Sequential Compression Device Airos Medical, Inc. | JOW |
| Jun 22, 2018 | K172779 | AIROS 8 Sequential Compression Device Airos Medical, Inc. | JOW |
| Jun 22, 2018 | K172770 | AIROS 6 Sequential Compression Device Airos Medical, Inc. | JOW |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||